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T6592ML133 hydrochloridePotassium Channel,KcsA,Inhibitor,inhibit,ML 133,ML-133 hydrochloride,ML133 hydroc
ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
价 格：￥电议型 号：T6592产 地：中国大陆
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T9242Dimethyl-d6 SulfoxideDimethyl-d-6 Sulfoxide,Dimethyld6 Sulfoxide,Dimethyl d6 Sulfoxide
Dimethyl-d6 Sulfoxide is a form in which hydrogen ("H") of dimethyl sulfoxide (DMSO, (CH3) 2S = O) is replaced by another isotope deuterium ("d"). Dimethyl-d6 Sulfoxide is a common solvent in nuclear magnetic resonance spectroscopy.
价 格：￥电议型 号：T9242产 地：中国大陆
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TN6792O-AcetylgalanthamineInhibitor,inhibit,OAcetylgalanthamine,Narcissus pseudonarcissus,acetylated alkal
The O-Acetylgalanthamine is a natural product that have been found in bulbs of Narcissus pseudonarcissu.
价 格：￥电议型 号：TN6792产 地：中国大陆
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T21792CGP 3466B maleate
Omigapil maleate is an orally bioavailable GAPDH nitrosylation inhibitor. Omigapil maleate abrogates Aβ1-42-induced tau acetylation, memory impairment, and locomotor dysfunction in mice. Omigapil maleate has the potential for the research of Alzheimer´s disease. Omigapil maleate (CGP3446B maleate) is a apoptosis inhibitor. Omigapil maleate can be used for the research of congenital muscular dystrophy (CMD).
价 格：￥电议型 号：T21792产 地：中国大陆
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T9258AficamtenCK3773274,CK-3773274,cardiac,CK-274,Myosin,cardiomyopathy,Inhibitor,CK 3773274,CK 274,hyper
Aficamten is a Next-Generation Cardiac Myosin Inhibitor for the Treatment of Hypertrophic Cardiomyopathy.
价 格：￥电议型 号：T9258产 地：中国大陆
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T8543KN-92 hydrochlorideInhibitor,derivative,experimental,inactive,KN-92,KN92 hydrochloride,KN92,inhibit,
KN-92 hydrochloride is an inactive derivative of KN-93. KN-93 is a selective Ca2+/calmodulin-dependent kinase II (CaMKII) inhibitor, competitively blocking CaM binding to the kinase with Ki of 370 nM.
价 格：￥电议型 号：T8543产 地：中国大陆
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T19676Tributyrinantiproliferative,fatty acid triglyceride,Inhibitor,proapoptotic,prodrug,inhibit,21920,Tri
Tributyrin (Glyceryl tributyrate), a neutral short-chain fatty acid triglyceride, is a stable and rapidly absorbed prodrug of Butyric Acid. Tributyrin diffuses through biological membranes and is metabolized by intracellular lipases, releasing effective butyrate directly into the cell in vivo. Tributyrin has potent proapoptotic, antiproliferative, and differentiation-inducing effects.
价 格：￥电议型 号：T19676产 地：中国大陆
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TP1928L1[Orn5]-URP acetate[Orn5] URP acetate,[Orn5]URP acetate
[Orn5]-URP acetate is an effective and selective Urotensin-II receptor (UT) antagonist (pEC50 = 7.24). [Orn5]-URP exhibits no agonist activity.
价 格：￥电议型 号：TP1928L1产 地：中国大陆
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T13926TigemonamTigemonam
Tigemonam is a monobactam. Tigemonam has potent activity against Gram-negative aerobic bacterial pathogens.
价 格：￥电议型 号：T13926产 地：中国大陆
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T9089FTO-IN-1mass,cancer,FTO,associated,enzyme,inhibit,FTOIN1,fat,obesity,Inhibitor,FTO IN 1
UUN44923 is a FTO inhibitor. It may be useful for treating diseases assocd. with FTO targets, obesity, metabolic syndrome (MS) , type 2 diabetes (T2D) , Alzheimer´s diseases, breast cancers, small- cell lung cancers, a human bone marrow striated muscle cancer, a pancreatic cancer, malignant glioblastoma and the like.
价 格：￥电议型 号：T9089产 地：中国大陆
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TP2322Lbeta-Neoendorphin acetate(77739-21-0 free base)betaNeoendorphin acetate(77739210 free base),beta Neo
beta-Neoendorphin acetate is an agonist of κ-opioid receptor
价 格：￥电议型 号：TP2322L产 地：中国大陆
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T39211PD 144418 oxalatePD 144418 oxalate
PD 144418 oxalate is a highly affinity, potent and selective sigma 1 (σ1) receptor ligand ( K i values of 0.08 nM and 1377 nM for σ1 and σ2 respectively). PD 144418 oxalate devoids of any significant affinity for other receptors, ion channels and enzymes. PD 144418 oxalate shows potential antipsychotic activity.
价 格：￥电议型 号：T39211产 地：中国大陆
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T40544NCGC00092410
NCGC00092410 is a glucocerebrosidase (GC) inhibitor with IC50 value of 31 nM. It can be used for the study of Gaucher disease caused by mutation of glucocerebrase gene.
价 格：￥电议型 号：T40544产 地：中国大陆
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T9262MAT2A inhibitor 4methionine,MAT2A inhibitor 4,FIDAS,inhibit,cancer,antineoplastic,dialkylaminostilbe
MAT2A inhibitor 4 is an inhibitor of the catalytic subunit of methionine S-adenosyltransferase-2 (MAT2A) and can be used for the research of cancer.
价 格：￥电议型 号：T9262产 地：中国大陆
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TN119216-Epivoacarpine16-Epivoacarpine,Inhibitor,16 Epivoacarpine,16Epivoacarpine,inhibit
16-Epivoacarpine is a natural product from Gelsemium elegans.
价 格：￥电议型 号：TN1192产 地：中国大陆
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T7927β-IononeApoptosis,inhibit,β-Ionone,β Ionone,βIonone,Inhibitor
β-lonone is an end-ring analog of β-carotenoids which widely distributed in fruit and vegetables,with anti-proliferative, anti-metastatic
价 格：￥电议型 号：T7927产 地：中国大陆
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T62929RLX-33
RLX-33 is a potent, selective and blood-brain barrier (BBB) penetrant antagonist of relaxin family peptide 3 (RXFP3, IC50=2.36 μM). RLX-33 also blocks relaxin-3-induced ERK1/2 phosphorylation, with IC50s of 7.82 and 13.86 μM for ERK1 and ERK2 phosphorylation, respectively. RLX-33 can inhibits the stimulation of food intake induced by the RXFP3-selective agonist R3/I5 in rats.
价 格：￥电议型 号：T62929产 地：中国大陆
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T9064LY3143921 hydrateLY-3143921 hydrate,LY3143921 hydrate
LY3143921 ((S)-Example 2) hydrate is an orally active CDC7 kinase inhibitor with broad in vitro anticancer activity [1].
价 格：￥电议型 号：T9064产 地：中国大陆
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TP1592LC-Reactive Protein (CRP) 174-185 acetateCReactive Protein (CRP) 174185 acetate,C Reactive Protein (C
C-Reactive Protein (CRP) 174-185 acetate is an acute phase serum protein synthesized in response to inflammatory cytokines, produces antitumor effects in animals. The fragment CRP (174-185) (RS-83277) shows similar activity by significantly enhancing the tumoricidal activity of human monocytes and alveolar macrophages in vitro.
价 格：￥电议型 号：TP1592L产 地：中国大陆
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T8092Taurohyodeoxycholic acid sodium salt hydrateTaurohyodeoxycholic acid sodium salt hydrate
Taurohyodeoxycholic acid sodium salt hydrate prevents apoptosis by blocking a calcium-mediated apoptotic pathway as well as caspase-12 activation.
价 格：￥电议型 号：T8092产 地：中国大陆
